Medical Writing Specialist
7 days ago
**About the Role**
We are seeking a highly skilled Medical Writing Specialist to join our team at LEE Fortrea Clinical Research Unit Limited. As a key member of our clinical operations team, you will be responsible for the compilation and publishing of high-complexity clinical documents for regulatory submissions.
Key Responsibilities
- Compile and publish clinical documents in accordance with regulatory submission standards, including electronic QC, PDF bookmarking, cross-references, and internal/external hyperlinking.
- Work closely with globally diverse teams to ensure clinical documents are developed in accordance with appropriate style guides and requirements for international regulatory publishing.
- Manage compiling and publishing projects, setting priorities, and ensuring deadlines are accomplished.
- Closely monitor study progress against plan and identify any significant variance and recommend actions to implement if timelines are not on target.
Requirements
- Minimum 2 years of experience as a Publisher in a medical writing or clinical department, either in CRO, Pharma, or Biotech environments.
- Master of Science or bachelor's degree in a biomedical, life sciences, or related discipline.
- Advanced experience with MS Office, especially Word processing skills (macros, templates, etc.) as well as Adobe Acrobat/DXC.
About Us
At LEE Fortrea Clinical Research Unit Limited, we empower our employees to shape their own career path. Whether you are passionate about the medical writing scientific side or aspire to be in leadership roles, we provide comprehensive training, management support, a network of SME's and KOL's, and opportunities to help you thrive.
We are actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.
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